A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv659013



Internal ID15395665
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:15669937..15719658hg38UCSC Ensembl
Innerchr19:15780747..15830468hg19UCSC Ensembl
Innerchr19:15641747..15691468hg18UCSC Ensembl
Innerchr19:15641747..15691468hg17UCSC Ensembl
Cytoband19p13.12
Allele length
AssemblyAllele length
hg3849722
hg1949722
hg1849722
hg1749722
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv516707
Supporting Variants
Samples
Known GenesCYP4F12
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv659013
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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